Evidence map›Paper›PMID 40186141›Full record

ArticleBMC urology2025

KIF14 plays a role in the regulation of the cell cycle and has implications for prognosis in clear cell renal cell carcinoma.

Jie Wang, Xuejia Lai, Zhijun Sun, Sike Feng, Bi Li, Hu Zhao

Abstract read
In one paragraph

Article in BMC urology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Jie Wang *Department of Urology, Ningbo Ninth Hospital, No.68, Xiangbei Road, Ningbo, Zhejiang, 315000, PR China. ddcsw000@stu.xmu.edu.cn.
Xuejia Lai *Department of Urology, Ningbo Ninth Hospital, No.68, Xiangbei Road, Ningbo, Zhejiang, 315000, PR China.
Zhijun SunDepartment of Urology, Ningbo Ninth Hospital, No.68, Xiangbei Road, Ningbo, Zhejiang, 315000, PR China.
Sike FengDepartment of Urology, Ningbo Ninth Hospital, No.68, Xiangbei Road, Ningbo, Zhejiang, 315000, PR China.
Bi LiDepartment of Urology, Ningbo Ninth Hospital, No.68, Xiangbei Road, Ningbo, Zhejiang, 315000, PR China.
Hu ZhaoDepartment of General Surgery, 900 Hospital of the Joint Logistics Support Force, 156 Xierhuan Road, Fuzhou, Fujian, 350025, PR China. zhaohubear@163.com.

Funding

Medical Science and Technology Project of Zhejiang Province 2023RC267
6 · The paper itself

Abstract

backgroundKinesin family member 14 (KIF14) is a significant multifunctional protein that has been linked to several malignancies. However, the varied expression profiles of KIF14 and its prognostic relevance in Clear cell renal cell carcinoma (ccRCC) have yet to be elucidated.

methodsPatients with ccRCC were obtained from The Cancer Genome Atlas (TCGA), Gene Expression Omnibus (GEO) and ArrayExpress databases. A comparison of KIF14 expression levels between ccRCC and normal tissues was conducted using the Wilcoxon rank sum test. Logistic regression analysis was subsequently employed to evaluate the relationship between KIF14 expression and clinicopathological features. Furthermore, Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) term analysis, gene set enrichment analysis (GSEA) and single sample gene set enrichment analysis (ssGSEA), as well as CIBERSORT, were utilized to elucidate the enriched pathways and functions linked to KIF14 and to quantify the level of immune cell infiltration. Kaplan-Meier analysis was conducted to assess the correlation between KIF14 expression and survival. Additionally, KIF14 expression was downregulated in A498 ccRCC cells, and their proliferation, expansion capacity, cell cycle, and apoptosis were assessed through CCK-8 assays, colony formation assays, 7-AAD staining, and Annexin V/PI staining, respectively.

resultsThe findings of this study demonstrate that KIF14 mRNA levels are notably increased in ccRCC. Furthermore, a positive association was observed between KIF14 expression and cancer stage, nodal metastasis, and the infiltration of various immune cells in ccRCC. High levels of KIF14 were also found to be indicative of poor survival outcomes among ccRCC patients. Knockdown of KIF14 in A498 cells resulted in reduced proliferation, diminished colony formation capacity, cell cycle arrest, increased apoptosis, and downregulation of CyclinD1 and CDK4.

conclusionsKIF14 down-regulates cell cycle proteins CyclinD1 and CDK4 to facilitate the proliferation of ccRCC cells, suggesting its potential as a therapeutic target and prognostic biomarker in ccRCC.

Indexed as

Carcinoma, Renal CellCell CycleKidney NeoplasmsKinesinsOncogene ProteinsCell Line, TumorCell ProliferationFemaleGene Expression Regulation, NeoplasticHumansMaleMiddle AgedPrognosisKIF14 protein, humanKinesinsOncogene ProteinsCell cycleClear cell renal cell carcinomaImmune infiltrationKIF14Proliferation

Identifiers

PMID40186141
PMCPMC11969952

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